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OpenTrials
Completed

NCT Number: NCT00237926

Comparing Aerobic to Resistance Training in Recovery From Cancer

The purpose of this study is to compare the health outcomes of a 12-week exercise program focused on aerobic training (using a treadmill) to a 12-week exercise program focused on resistance training (using Thera-Bands) in sedentary patients within 6 months of completing treatment for cancer.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Brooke Army Medical Center

Fort Sam Houston, Texas, 78234, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • have a biopsy-proven cancer diagnosis
  • be within six months of having completed chemotherapy or radiation therapy for treatment for cancer as determined by the primary physician
  • be ambulatory but sedentary (i. e., has not followed an exercise regimen of a minimum of 3 times per week for at least 20 minutes each session over the previous six weeks)
  • have an Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 asymptomatic) or 1 (symptomatic, fully ambulatory)
  • be at least 18 years old
  • be able to read and speak English
  • have a medical statement from either the patient's primary care provider or the primary oncologist indicating that participation in the program is not medically contraindicated

Exclusion criteria

  • following an exercise regimen a minimum of 3 times per week for at least 20 minutes each session within the previous 6 weeks
  • bone or joint destruction that could be aggravated with exercise
  • severe cognitive impairment identified by either the patient's medical care provider or by the study team
  • neuropathy-sensory common toxicity criteria (CTC) grade 3 (sensory loss or paresthesia interfering with activities of daily living) or grade 4 (permanent sensory loss that interferes with function) peripheral neuropathy

Treatment and study plan

Exercise

Behavioral

aerobic or resistance training

Primary outcomes

  1. quality of life

    Time frame: 12-weeks

Secondary outcomes

  1. exercise tolerance

    Time frame: 12-weeks

Sponsors and collaborators

Lead sponsor

TriService Nursing Research Program

Other

Registry information

Important dates

Study start
2005
Primary completion
2008
First posted
Oct 13, 2005
Registry last updated
Aug 1, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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